A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040824



Internal ID19130043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98570081..98590299hg38UCSC Ensembl
Innerchr14:99036418..99056636hg19UCSC Ensembl
Innerchr14:98106171..98126389hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3820219
hg1920219
hg1820219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1967n100
Supporting Variantsnssv3532705, nssv3532704, nssv3532706
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040824
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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